Found: 48
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Are mouse lens epithelial cells more sensitive to γ-irradiation than lymphocytes?
- Published in:
- Radiation & Environmental Biophysics, 2013, v. 52, n. 2, p. 279, doi. 10.1007/s00411-012-0451-8
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- Publication type:
- Article
A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains.
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- Genome Biology, 2013, v. 14, n. 7, p. R82, doi. 10.1186/gb-2013-14-7-r82
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- Publication type:
- Article
Haemophilia A: from mutation analysis to new therapies.
- Published in:
- Nature Reviews Genetics, 2005, v. 6, n. 6, p. 488, doi. 10.1038/nrg1617
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- Publication type:
- Article
The genetic and molecular basis of congenital eye defects.
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- Nature Reviews Genetics, 2003, v. 4, n. 11, p. 876, doi. 10.1038/nrg1202
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- Publication type:
- Article
Mutations within the cGMP-binding domain of CNGA1 causing autosomal recessive retinitis pigmentosa in human and animal model.
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- Cell Death Discovery, 2022, v. 8, n. 1, p. 1, doi. 10.1038/s41420-022-01185-0
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- Publication type:
- Article
Peroxidasin is essential for eye development in the mouse.
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- Human Molecular Genetics, 2014, v. 23, n. 21, p. 5597, doi. 10.1093/hmg/ddu274
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- Publication type:
- Article
Permanent neonatal diabetes in INS(C94Y) transgenic pigs.
- Published in:
- 2013
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- Publication type:
- journal article
Permanent Neonatal Diabetes in INS<sup>C94Y</sup> Transgenic Pigs.
- Published in:
- Diabetes, 2013, v. 62, n. 5, p. 1505, doi. 10.2337/db12-1065
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- Publication type:
- Article
Application of WES towards Molecular Investigation of Congenital Cataracts: Identification of Novel Alleles and Genes in a Hospital-Based Cohort of South India.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 24, p. 9569, doi. 10.3390/ijms21249569
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- Publication type:
- Article
Crybb2 Mutations Consistently Affect Schizophrenia Endophenotypes in Mice.
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- Molecular Neurobiology, 2019, v. 56, n. 6, p. 4215, doi. 10.1007/s12035-018-1365-5
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- Publication type:
- Article
<italic>Fgf9</italic><sup><italic>Y162C</italic></sup> Mutation Alters Information Processing and Social Memory in Mice.
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- Molecular Neurobiology, 2018, v. 55, n. 6, p. 4580, doi. 10.1007/s12035-017-0659-3
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- Publication type:
- Article
Laboratory mouse housing conditions can be improved using common environmental enrichment without compromising data.
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- PLoS Biology, 2018, v. 16, n. 4, p. 1, doi. 10.1371/journal.pbio.2005019
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- Publication type:
- Article
Mutation in the mouse histone gene Hist2h3c1 leads to degeneration of the lens vesicle and severe microphthalmia.
- Published in:
- Acta Ophthalmologica (1755375X), 2019, v. 97, p. N.PAG, doi. 10.1111/j.1755-3768.2019.8117
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- Publication type:
- Article
Relative roles of the different Pax6 domainsfor pancreatic alpha cell development.
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- BMC Developmental Biology, 2010, v. 10, p. 39, doi. 10.1186/1471-213X-10-39
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- Publication type:
- Article
Crybb2 coding for βB2-crystallin affects sensorimotor gating and hippocampal function.
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- Mammalian Genome, 2013, v. 24, n. 9/10, p. 333, doi. 10.1007/s00335-013-9478-7
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- Publication type:
- Article
Lens density tracking in mice by Scheimpflug imaging.
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- Mammalian Genome, 2013, v. 24, n. 7/8, p. 295, doi. 10.1007/s00335-013-9470-2
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- Publication type:
- Article
Longitudinal fundus and retinal studies with SD-OCT: a comparison of five mouse inbred strains.
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- Mammalian Genome, 2013, v. 24, n. 5/6, p. 198, doi. 10.1007/s00335-013-9457-z
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- Publication type:
- Article
Variations of eye size parameters among different strains of mice.
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- Mammalian Genome, 2006, v. 17, n. 8, p. 851, doi. 10.1007/s00335-006-0019-5
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- Publication type:
- Article
Mapping of a novel MEN-like syndrome locus to rat Chromosome 4.
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- Mammalian Genome, 2004, v. 15, n. 2, p. 135, doi. 10.1007/s00335-003-3027-8
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- Publication type:
- Article
V76D mutation in a conserved gD-crystallin region leads to dominant cataracts in mice.
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- Mammalian Genome, 2002, v. 13, n. 8, p. 452, doi. 10.1007/s00335-002-3021-6
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- Publication type:
- Article
The Pathologic Effect of a Novel Neomorphic Fgf9<sup>Y162C</sup> Allele Is Restricted to Decreased Vision and Retarded Lens Growth.
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- PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0023678
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- Publication type:
- Article
Mouse models for microphthalmia, anophthalmia and cataracts.
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- Human Genetics, 2019, v. 138, n. 8/9, p. 1007, doi. 10.1007/s00439-019-01995-w
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- Publication type:
- Article
Standardized, systemic phenotypic analysis of Slc12a1<sup>I299F</sup> mutant mice.
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- Journal of Biomedical Science, 2014, v. 21, n. 1, p. 1, doi. 10.1186/s12929-014-0068-0
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- Publication type:
- Article
Visual capabilities and cortical maps in BALB/c mice.
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- European Journal of Neuroscience, 2012, v. 36, n. 6, p. 2801, doi. 10.1111/j.1460-9568.2012.08195.x
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- Publication type:
- Article
Altered aggregation properties of mutant ?-crystallins cause inherited cataract.
- Published in:
- EMBO Journal, 2002, v. 21, n. 22, p. 6005, doi. 10.1093/emboj/cdf609
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- Publication type:
- Article
Features of Age-Related Macular Degeneration in the General Adults and Their Dependency on Age, Sex, and Smoking: Results from the German KORA Study.
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- PLoS ONE, 2016, v. 11, n. 11, p. 1, doi. 10.1371/journal.pone.0167181
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- Publication type:
- Article
Agonistic and Antagonistic Action of AP2, Msx2, Pax6, Prox1 and Six3 in the Regulation of Sox2 Expression.
- Published in:
- Ophthalmic Research, 2005, v. 37, n. 6, p. 301, doi. 10.1159/000087774
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- Publication type:
- Article
The Cryner Element in the Murine γ-Crystallin Promoters Interacts with Lens Proteins.
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- Ophthalmic Research, 1997, v. 29, n. 3, p. 161, doi. 10.1159/000268011
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- Publication type:
- Article
Cataract Mutations as a Tool for Developmental Geneticists.
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- Ophthalmic Research, 1996, v. 28, n. S1, p. 8, doi. 10.1159/000267936
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- Publication type:
- Article
Oxidative Stress and Inherited Cataracts in Mice.
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- Ophthalmic Research, 1989, v. 21, n. 6, p. 414, doi. 10.1159/000266931
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- Publication type:
- Article
Antagonistic action of Six3 and Prox1 at the γ-crystallin promoter.
- Published in:
- Nucleic Acids Research, 2001, v. 29, n. 2, p. 515, doi. 10.1093/nar/29.2.515
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- Publication type:
- Article
Common eye diseases in older adults of southern Germany: results from the KORA-Age study.
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- Age & Ageing, 2017, v. 46, n. 3, p. 481, doi. 10.1093/ageing/afw234
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- Publication type:
- Article
Characterization of ex vivo cultured neuronal- and glial- like cells from human idiopathic epiretinal membranes.
- Published in:
- BMC Ophthalmology, 2014, v. 14, n. 1, p. 166, doi. 10.1186/1471-2415-14-165
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- Publication type:
- Article
Visualizing corticotropin-releasing hormone receptor type 1 expression and neuronal connectivities in the mouse using a novel multifunctional allele.
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- Journal of Comparative Neurology, 2012, v. 520, n. 14, p. 3150, doi. 10.1002/cne.23082
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- Publication type:
- Article
Complex Long-term Effects of Radiation on Adult Mouse Behavior.
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- Radiation Research, 2022, v. 197, n. 1, p. 67, doi. 10.1667/RADE-20-00281.1
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- Publication type:
- Article
On the Nature of Murine Radiation-Induced Subcapsular Cataracts: Optical Coherence Tomography-Based Fine Classification, In Vivo Dynamics and Impact on Visual Acuity.
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- Radiation Research, 2022, v. 197, n. 1, p. 7, doi. 10.1667/RADE-20-00163.1
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- Publication type:
- Article
Peroxidasin contributes to lung host defense by direct binding and killing of gram-negative bacteria.
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- PLoS Pathogens, 2018, v. 14, n. 5, p. 1, doi. 10.1371/journal.ppat.1007026
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- Publication type:
- Article
Mutation in Intron 6 of the Hamster Mitf Gene Leads to Skipping of the Subsequent Exon and Creates a Novel Animal Model for the Human Waardenburg Syndrome Type II.
- Published in:
- Genetics, 2003, v. 164, n. 3, p. 1035, doi. 10.1093/genetics/164.3.1035
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- Publication type:
- Article
Ethylnitrosourea-Induced Base Pair Substitution Affects Splicing of the Mouse γE-Crystallin Encoding Gene Leading to the Expression of a Hybrid Protein and to a Cataract.
- Published in:
- Genetics, 2002, v. 161, n. 4, p. 1633, doi. 10.1093/genetics/161.4.1633
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- Publication type:
- Article
Ethylnitrosourea-Induced Mutation in Mice Leads to the Expression of a Novel Protein in the Eye...
- Published in:
- Genetics, 2001, v. 157, n. 3, p. 1313, doi. 10.1093/genetics/157.3.1313
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- Publication type:
- Article
Hereditary Lactate Dehydrogenase A-Subunit Deficiency as Cause of Early Postimplantation Death of Homozygotes in Mus musculus.
- Published in:
- Genetics, 1992, v. 131, n. 2, p. 413
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- Publication type:
- Article
Polymorphisms in CRYBB2 encoding βB2-crystallin are associated with antisaccade performance and memory function.
- Published in:
- Translational Psychiatry, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41398-020-0791-0
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- Publication type:
- Article
Isolation and embryonic expression of the novel mouse gene , the homologue of , a candidate gene for the Miller-Dieker syndrome.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 4, p. 697, doi. 10.1093/hmg/8.4.697
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- Publication type:
- Article
Allelic loss of chromosomes 8 and 19 in MENX-associated rat pheochromocytoma.
- Published in:
- International Journal of Cancer, 2010, v. 126, n. 10, p. 2362, doi. 10.1002/ijc.24925
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- Publication type:
- Article
Cancer-retina antigens as potential paraneoplastic antigens in melanoma-associated retinopathy.
- Published in:
- International Journal of Cancer, 2009, v. 124, n. 1, p. 140, doi. 10.1002/ijc.23909
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- Publication type:
- Article
New Mutation in the Mouse Xpd/Ercc2 Gene Leads to Recessive Cataracts.
- Published in:
- PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0125304
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- Publication type:
- Article
Erratum to: Mouse models of cataract.
- Published in:
- 2010
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- Publication type:
- Erratum
Mouse models of cataract.
- Published in:
- Journal of Genetics, 2009, v. 88, n. 4, p. 469, doi. 10.1007/s12041-009-0066-2
- By:
- Publication type:
- Article